For one of our single‑sponsor partnerships we are currently looking for a Site Activation Manager or Specialist here in Switzerland.

This role is accountable for performance and compliance for assigned protocols in Switzerland in compliance with ICH/GCP and country regulations, sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight the person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure site readiness.

Job Responsibilities

• Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA).
• Oversees and tracks clinical research‑related payments. Payment reconciliation at study close‑out. Oversees FCPA, DPS/OFAC, and maintenance of financial systems.
• Executes and oversees clinical trial country submiss...